Shibata T, Perparim K, Sumie A, Ishii T, Tomo T, Tashiro T, Nasu M, Yasumori R
Second Department of Internal Medicine, Oita Medical University, Japan.
Nihon Jinzo Gakkai Shi. 1993 Jan;35(1):83-8.
We report the case of a 67-year-old man with allergic granulomatosis and angiitis (AGA; Churg-Strauss syndrome) who developed nephrotic syndrome during his clinical course and demonstrated membranous nephropathy on renal necropsy by electron microscopy. Following the development of symptoms of bronchial asthma accompanied by eosinophilia and mononeuritis multiplex, transbronchial lung biopsy confirmed a diagnosis of AGA. The patient died of pneumonia and disseminated intravascular coagulopathy, but necropsy revealed severe tubulo-interstitial damage with neutrophilic infiltration and, in half of the glomeruli, mesangial proliferation with subepithelial dense deposits. This paper thus describes a rare case of AGA complicated by a secondary type of stage I membranous nephropathy.
我们报告了一例67岁男性患变应性肉芽肿性血管炎(AGA;Churg-Strauss综合征)的病例,该患者在临床过程中出现肾病综合征,肾尸检经电子显微镜检查显示为膜性肾病。在出现伴有嗜酸性粒细胞增多和多发性单神经炎的支气管哮喘症状后,经支气管肺活检确诊为AGA。患者死于肺炎和弥散性血管内凝血,但尸检显示有严重的肾小管间质损伤伴中性粒细胞浸润,且半数肾小球有系膜增生和上皮下致密沉积物。因此,本文描述了一例罕见的AGA并发继发性I期膜性肾病的病例。